Global Supplier Quality Lead Auditor

Philips

Colorado Springs, CO, US
Base: $94,000 to $168,000 depending on location; b...
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7+ years experience in quality engineering
External supplier audits in medical device industry
Formal training in iso 13485 and iso 9001
** Philips is seeking a Global Supplier Quality Lead Auditor to conduct external audits of suppliers in the medical device industry, ensuring compliance with quality management systems and regulatory standards. The role requires significant experience in quality engineering and supplier auditing, along with strong communication skills and the ability to work both independently and collaboratively. **

Job Summary

  • This role is critical in ensuring that the supply base maintains robust, compliant, and effective Quality Management Systems aligned with ISO 13485 and ISO 9001.
  • The Lead Auditor will evaluate supplier processes, identify risks, drive corrective action, and support qualification activities essential to patient safety.
  • Employees are eligible to participate in a comprehensive Philips Total Rewards benefits program which includes generous PTO, 401k match, and stock purchase plans.

Matching Summary

Match Score: 75

** Philips is seeking a Global Supplier Quality Lead Auditor to conduct external audits of suppliers in the medical device industry, ensuring compliance with quality management systems and regulatory standards. The role requires significant experience in quality engineering and supplier auditing, along with strong communication skills and the ability to work both independently and collaboratively. **

Salary

Base: $94,000 to $168,000 depending on location; Bonus/Equity: Annual incentive bonus, sales commission, or long-term incentives may be offered; Benefits: Generous PTO, 401k up to 7% match, HSA, stock purchase plan, education reimbursement

Skills & Requirements

Must-have

  • 7+ years experience in quality engineering
  • External supplier audits in medical device industry
  • Formal training in ISO 13485 and ISO 9001
  • Certified Lead Auditor through recognized program
  • Proficiency with audit management systems

Nice-to-have

  • Strong understanding of medical device QMS
  • Ability to assess complex manufacturing processes
  • Excellent communication and negotiation skills
  • Experience with ISO 17025 standards
  • Master's degree in relevant field

Key Requirements

  • Bachelor's degree in Engineering or equivalent
  • 7+ years of relevant experience
  • Certified Lead Auditor (IRCA, RAB-QSA, ASQ, BSI, TUV)
  • US work authorization required without sponsorship
  • Willingness to travel up to 50%

Work Rights

Must have US work authorization

Tailored Resume

Cover Letter